Division of Hematology/Oncology, Department of Internal Medicine V, and.
Amyloidosis Center, Heidelberg University Hospital, Germany.
Blood. 2020 Apr 30;135(18):1517-1530. doi: 10.1182/blood.2019003633.
Daratumumab has shown promising first results in systemic amyloid light-chain (AL) amyloidosis. We analyzed a consecutive series of 168 patients with advanced AL receiving either daratumumab/dexamethasone (DD, n = 106) or daratumumab/bortezomib/dexamethasone (DVD, n = 62). DD achieved a remission rate (RR) of 64% and a very good hematologic remission (VGHR) rate of 48% after 3 months. Median hematologic event-free survival (hemEFS) was 11.8 months and median overall survival (OS) was 25.6 months. DVD achieved a 66% RR and a 55% VGHR rate. Median hemEFS was 19.1 months and median OS had not been reached. Cardiac organ responses were noted in 22% with DD and 26% with DVD after 6 months. Infectious complications were common (Common Terminology Criteria [CTC] grade 3/4: DD 16%, DVD 18%) and likely related to a high rate of lymphocytopenia (CTC grade 3/4: DD 20%, DVD 17%). On univariable analysis, hyperdiploidy and gain 1q21 conferred an adverse factor for OS and hemEFS with DD, whereas translocation t(11;14) was associated with a better hemEFS. N-terminal prohormone of brain natriuretic peptide >8500 ng/L could not be overcome for survival with each regimen. Multivariable Cox regression analysis revealed plasma cell dyscrasia (difference between serum free light chains [dFLC]) >180 mg/L as an overall strong negative prognostic factor. Additionally, nephrotic-range albuminuria with an albumin-to-creatinine-ratio (ACR) >220 mg/mmol was a significantly adverse factor for hemEFS (hazard ratio, 2.1 and 3.1) with DD and DVD. Daratumumab salvage therapy produced good results and remission rates challenging any therapy in advanced AL. Outcome is adversely influenced by the activity of the underlying plasma cell dyscrasia (dFLC) and nephrotic-range albuminuria (ACR).
达雷妥尤单抗在系统性轻链淀粉样变性(AL)淀粉样变性中显示出有希望的初步结果。我们分析了连续 168 例接受达雷妥尤单抗/地塞米松(DD,n=106)或达雷妥尤单抗/硼替佐米/地塞米松(DVD,n=62)治疗的晚期 AL 患者的系列。DD 在 3 个月后达到缓解率(RR)64%和非常好的血液学缓解(VGHR)率 48%。中位血液学无事件生存(hemEFS)为 11.8 个月,中位总生存(OS)未达到。DVD 达到 66%的 RR 和 55%的 VGHR 率。中位 hemEFS 为 19.1 个月,中位 OS 尚未达到。DD 和 DVD 分别在 6 个月后观察到 22%和 26%的心脏器官反应。感染并发症常见(常见不良事件通用术语标准[CTC]3/4 级:DD 16%,DVD 18%),可能与淋巴细胞减少症发生率高有关(CTC 3/4 级:DD 20%,DVD 17%)。单变量分析显示,超二倍体和 1q21 增益是 DD 患者 OS 和 hemEFS 的不利因素,而 t(11;14)易位与更好的 hemEFS 相关。用每种方案都无法克服脑钠肽前体 N 端(NT-proBNP)>8500ng/L 来提高生存率。多变量 Cox 回归分析显示浆细胞增生不良(血清游离轻链[dFLC]差值)>180mg/L 是总体上强烈的负预后因素。此外,DD 和 DVD 中,白蛋白/肌酐比(ACR)>220mg/mmol 的肾病范围白蛋白尿是 hemEFS 的显著不利因素(危险比,2.1 和 3.1)。达雷妥尤单抗挽救疗法产生了良好的结果和缓解率,挑战了晚期 AL 的任何治疗。疾病的活动度(dFLC)和肾病范围白蛋白尿(ACR)对预后有不利影响。